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A Study of a Glaucoma Therapy to Treat Open-Angle Glaucoma or Ocular Hypertension
This study has been completed.
First Received: April 10, 2006   Last Updated: February 29, 2008   History of Changes
Sponsor: Alcon Research
Information provided by: Alcon Research
ClinicalTrials.gov Identifier: NCT00314158
  Purpose

The purpose of this study is to determine whether a glaucoma therapy is safe and effective in treating patients with open-angle glaucoma or ocular hypertension.


Condition Intervention Phase
Open-Angle Glaucoma
Ocular Hypertension
Drug: Brinzolamide 1%/Timolol 0.5%, Brinzolamide 1%, Timolol 0.5%
Phase III

Study Type: Interventional
Study Design: Treatment, Randomized, Double-Blind, Active Control, Parallel Assignment, Safety/Efficacy Study

Resource links provided by NLM:

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Over 18 with open-angle glaucoma

Exclusion Criteria:

  • Under 18
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00314158

Locations
United States, Texas
United States Investigative Sites
Fort Worth, Texas, United States, 76134
Sponsors and Collaborators
Alcon Research
  More Information

No publications provided

Study ID Numbers: C-05-24
Study First Received: April 10, 2006
Last Updated: February 29, 2008
ClinicalTrials.gov Identifier: NCT00314158     History of Changes
Health Authority: United States: Food and Drug Administration

Additional relevant MeSH terms:
Neurotransmitter Agents
Molecular Mechanisms of Pharmacological Action
Adrenergic Agents
Brinzolamide
Eye Diseases
Physiological Effects of Drugs
Vascular Diseases
Enzyme Inhibitors
Cardiovascular Agents
Antihypertensive Agents
Pharmacologic Actions
Carbonic Anhydrase Inhibitors
Glaucoma
Therapeutic Uses
Glaucoma, Open-Angle
Adrenergic beta-Antagonists
Cardiovascular Diseases
Adrenergic Antagonists
Anti-Arrhythmia Agents
Timolol
Hypertension
Ocular Hypertension

ClinicalTrials.gov processed this record on November 25, 2009